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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1533149Generated: November 3, 2026

Methanol → HCID 22707666, compound

https://huagongshe.com/reaction/1533149

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantHCID 22707383HCID 22707383—
SolventDichloromethaneHCID 6344—
ProductHCID 22707666HCID 2270766634%

Reaction Steps

To a solution of 514.0 mg (1.26 mmol) of N-(4-aminophenyl)-4-(6,7-dimethoxy-4-quinazolinyl)-1-piperazinecarboxamide obtained in Example 221 in 10 ml of dichloromethane were added 0.18 ml (1.89 mmol) of acetic anhydride and 0.53 ml (3.78 mmol) of triethylamine under ice-cooling. After the resulting mixture was stirred overnight at room temperature, 0.18 ml (1.89 mmol) of acetic anhydride and 0.53 ml (3.78 mmol) of triethylamine were added thereto, followed by overnight stirring. To the reaction mixture was added methanol and the solvent was evaporated. Then, the residue was; purified by silica gel chromatography to give the desired compound as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06207667B1
Source datasetuspto-grants-2001_03
ORD IDord-8d32470394b64f46bfb06a5ed9b9338c
Source noteuspto-grants-2001_03